Antimicrobial metabolites from a marine-derived Actinomycete Streptomyces sp. G278

被引:17
作者
Duc Tuan Cao [1 ,2 ,3 ,4 ]
Van Hieu Tran [1 ,2 ]
Van Nam Vu [1 ,2 ]
Huong Doan Thi Mai [1 ,2 ,3 ]
Thi Hong Minh Le [1 ,2 ]
Thi Quyen Vu [1 ,2 ]
Hung Huy Nguyen [5 ]
Van Minh Chau [1 ,2 ]
Van Cuong Pham [1 ,2 ,3 ]
机构
[1] Vietnam Acad Sci & Technol, Adv Ctr Bioorgan Chem, Inst Marine Biochem, Hanoi, Vietnam
[2] Acad Sci & Technol, Hanoi, Vietnam
[3] VAST, Fac Chem, Grad Univ Sci & Technol, Hanoi, Vietnam
[4] Haiphong Univ Med & Pharm, Fac Pharm, Haiphong, Vietnam
[5] VNU Univ Sci, Fac Chem, Hanoi, Vietnam
关键词
Streptomyces sp; G278; 2; 5-Bis(5-tert-butyl-2-benzoxazolyl)thiophene; 2-methyl-3-pyridinol; actinomycetes; antibacterial; POLY(ETHYLENE-TEREPHTHALATE); BACTERIUM; PHTHALATE; ESTERS; C-13;
D O I
10.1080/14786419.2018.1468331
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Analysis of an antimicrobial extract prepared from culture broth of the marine-derived actinomycete Streptomyces sp. G278 led to the isolation of ten compounds, 1-10. Two compounds, 2,5-Bis(5-tert-butyl-2-benzoxazolyl)thiophene (1), and 3-hydroxyl-2-methylpyridine (2) were isolated from a natural source for the first time. The structures of the isolated compounds were established by their spectral data analysis, including mass spectrometry, 1D-NMR, 2D-NMR, and X-ray crystallographic analysis in case of compound 3. All isolated compounds were evaluated for their antimicrobial activity against a panel of clinically significant microorganisms. Compounds 1 and 3 selectively inhibited Enterococcus faecalis (MIC: 256 mu g/mL). Compound 2 was found to have antibacterial and antifungal activity against Escherichia coli (MIC: 64 mu g/mL), Salmonella enterica (MIC: 256 mu g/mL), Staphylococcus aureus (MIC: 256 mu g/mL), Enterococcus faecalis (MIC: 256 mu g/mL), and Candida albicans (MIC: 64 mu g/mL). Except for compounds 9 and 10, the other known metabolites (4-8) also exhibited antimicrobial activity.
引用
收藏
页码:3223 / 3230
页数:8
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